Your search returned 3 results.

Results
	1.	Phenotypic expansion in [electronic resource] by Wang, Xia Posey, Jennifer E Rosenfeld, Jill A Bacino, Carlos A Scaglia, Fernando Immken, LaDonna Harris, Jill M Hickey, Scott E Mosher, Theresa M Slavotinek, Anne Zhang, Jing Beuten, Joke Leduc, Magalie S He, Weimin Vetrini, Francesco Walkiewicz, Magdalena A Bi, Weimin Xiao, Rui Liu, Pengfei Shao, Yunru Gezdirici, Alper Gulec, Elif Y Jiang, Yunyun Darilek, Sandra A Hansen, Adam W Khayat, Michael M Pehlivan, Davut Piard, Juliette Muzny, Donna M Hanchard, Neil Belmont, John W Van Maldergem, Lionel Gibbs, Richard A Eldomery, Mohammad K Akdemir, Zeynep C Adesina, Adekunle M Chen, Shan Lee, Yi-Chien Lee, Brendan Lupski, James R Eng, Christine M Xia, Fan Yang, Yaping Graham, Brett H Moretti, Paolo Publication details: Annals of clinical and translational neurology Oct 2018 In: Annals of clinical and translational neurology vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. [electronic resource] by Vetrini, Francesco McKee, Shane Rosenfeld, Jill A Suri, Mohnish Lewis, Andrea M Nugent, Kimberly Margaret Roeder, Elizabeth Littlejohn, Rebecca O Holder, Sue Zhu, Wenmiao Alaimo, Joseph T Graham, Brett Harris, Jill M Gibson, James B Pastore, Matthew McBride, Kim L Komara, Makanko Al-Gazali, Lihadh Al Shamsi, Aisha Fanning, Elizabeth A Wierenga, Klaas J Scott, Daryl A Ben-Neriah, Ziva Meiner, Vardiella Cassuto, Hanoch Elpeleg, Orly Holder, J Lloyd Burrage, Lindsay C Seaver, Laurie H Van Maldergem, Lionel Mahida, Sonal Soul, Janet S Marlatt, Margaret Matyakhina, Ludmila Vogt, Julie Gold, June-Anne Park, Soo-Mi Varghese, Vinod Lampe, Anne K Kumar, Ajith Lees, Melissa Holder-Espinasse, Muriel McConnell, Vivienne Bernhard, Birgitta Blair, Ed Harrison, Victoria Muzny, Donna M Gibbs, Richard A Elsea, Sarah H Posey, Jennifer E Bi, Weimin Lalani, Seema Xia, Fan Yang, Yaping Eng, Christine M Lupski, James R Liu, Pengfei Producer: 20190613 In: Genome medicine vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome. [electronic resource] by Vetrini, Francesco McKee, Shane Rosenfeld, Jill A Suri, Mohnish Lewis, Andrea M Nugent, Kimberly Margaret Roeder, Elizabeth Littlejohn, Rebecca O Holder, Sue Zhu, Wenmiao Alaimo, Joseph T Graham, Brett Harris, Jill M Gibson, James B Pastore, Matthew McBride, Kim L Komara, Makanko Al-Gazali, Lihadh Al Shamsi, Aisha Fanning, Elizabeth A Wierenga, Klaas J Scott, Daryl A Ben-Neriah, Ziva Meiner, Vardiella Cassuto, Hanoch Elpeleg, Orly Lloyd Holder, J Burrage, Lindsay C Seaver, Laurie H Van Maldergem, Lionel Mahida, Sonal Soul, Janet S Marlatt, Margaret Matyakhina, Ludmila Vogt, Julie Gold, June-Anne Park, Soo-Mi Varghese, Vinod Lampe, Anne K Kumar, Ajith Lees, Melissa Holder-Espinasse, Muriel McConnell, Vivienne Bernhard, Birgitta Blair, Ed Harrison, Victoria Muzny, Donna M Gibbs, Richard A Elsea, Sarah H Posey, Jennifer E Bi, Weimin Lalani, Seema Xia, Fan Yang, Yaping Eng, Christine M Lupski, James R Liu, Pengfei Publication details: Genome medicine 03 2019 In: Genome medicine vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)